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Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis

S‐aryl phosphorothioates are privileged motifs in pharmaceuticals, agrochemicals, and catalysts; yet, the challenge of devising a straightforward synthetic route to enantioenriched S‐aryl phosphorothioates has remained unsolved to date. We demonstrate herein the first direct C−SP(=O)(OR′)(OR′′) coup...

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Autores principales: Chen, Xiang‐Yu, Pu, Maoping, Cheng, Hong‐Gang, Sperger, Theresa, Schoenebeck, Franziska
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771726/
https://www.ncbi.nlm.nih.gov/pubmed/31190467
http://dx.doi.org/10.1002/anie.201906063
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author Chen, Xiang‐Yu
Pu, Maoping
Cheng, Hong‐Gang
Sperger, Theresa
Schoenebeck, Franziska
author_facet Chen, Xiang‐Yu
Pu, Maoping
Cheng, Hong‐Gang
Sperger, Theresa
Schoenebeck, Franziska
author_sort Chen, Xiang‐Yu
collection PubMed
description S‐aryl phosphorothioates are privileged motifs in pharmaceuticals, agrochemicals, and catalysts; yet, the challenge of devising a straightforward synthetic route to enantioenriched S‐aryl phosphorothioates has remained unsolved to date. We demonstrate herein the first direct C−SP(=O)(OR′)(OR′′) coupling of diverse and chiral phosphorothioate salts with aryl iodides, enabled by an air‐ and moisture‐stable Pd(I) dimer. Our mechanistic and computational data suggest distinct dinuclear Pd(I) catalysis to be operative, which allows for operationally simple couplings with broad scope and full retention of stereochemistry.
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spelling pubmed-67717262019-10-07 Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis Chen, Xiang‐Yu Pu, Maoping Cheng, Hong‐Gang Sperger, Theresa Schoenebeck, Franziska Angew Chem Int Ed Engl Communications S‐aryl phosphorothioates are privileged motifs in pharmaceuticals, agrochemicals, and catalysts; yet, the challenge of devising a straightforward synthetic route to enantioenriched S‐aryl phosphorothioates has remained unsolved to date. We demonstrate herein the first direct C−SP(=O)(OR′)(OR′′) coupling of diverse and chiral phosphorothioate salts with aryl iodides, enabled by an air‐ and moisture‐stable Pd(I) dimer. Our mechanistic and computational data suggest distinct dinuclear Pd(I) catalysis to be operative, which allows for operationally simple couplings with broad scope and full retention of stereochemistry. John Wiley and Sons Inc. 2019-07-09 2019-08-12 /pmc/articles/PMC6771726/ /pubmed/31190467 http://dx.doi.org/10.1002/anie.201906063 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Communications
Chen, Xiang‐Yu
Pu, Maoping
Cheng, Hong‐Gang
Sperger, Theresa
Schoenebeck, Franziska
Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis
title Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis
title_full Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis
title_fullStr Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis
title_full_unstemmed Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis
title_short Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd(I) Catalysis
title_sort arylation of axially chiral phosphorothioate salts by dinuclear pd(i) catalysis
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771726/
https://www.ncbi.nlm.nih.gov/pubmed/31190467
http://dx.doi.org/10.1002/anie.201906063
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